{Reference Type}: Case Reports
{Title}: A rare primary sacral glomus tumor presenting as intradural-extramedullary tumor: A Case report and review of literature.
{Author}: Varshney R;Singh P;Deshpande S;Yadav S;
{Journal}: Surg Neurol Int
{Volume}: 15
{Issue}: 0
{Year}: 2024
暂无{DOI}: 10.25259/SNI_261_2024
{Abstract}: <B>UNASSIGNED: </B>Glomus tumors are very infrequent in the spine where they can grow intraosseously at any level. We were able to identify only eight such cases in the literature, with only one occurring in the sacrum. Here, a 48-year-old male with sacral S1/S2 radiculopathy was found to have a rare glomangioma/glomus tumor of the sacral region.<BR><B>UNASSIGNED: </B>A 48-year-old male presented with left-sided S2 radiculopathy characterized by left lower extremity weakness/paresis. The magnetic resonance showed an intradural extramedullary mass measuring 1.8 × 1.9 × 4.3 cm at S1-S2 extending through the left foramen, inhomogeneously enhanced with contrast. He underwent an S1-S2 durotomy with gross total excision of the mass. Pathologically, it proved to be a glomus tumor. Two months postoperatively, he ambulated without the support and demonstrated no tumor recurrence at 1 postoperative year.<BR><B>UNASSIGNED: </B>Glomus tumors involving the sacral region are rare and can be successfully excised resulting in good clinical outcomes.